Ge(IV)-citrate complex formation:: synthesis and structural characterisation of GeCl4(bipy) and GeCl(bipy)(Hcit) (bipy=2,2′-bipyridine, H4cit = citric acid)

被引:35
|
作者
Willey, GR [1 ]
Somasunderam, U [1 ]
Aris, DR [1 ]
Errington, W [1 ]
机构
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
citrate complexes; germanium complexes; crystal structures;
D O I
10.1016/S0020-1693(01)00358-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The adduct [GeCl4(bipy)] (I), obtained by direct treatment of the parent halide with 2,2'-bipyridine (bipy), reacts with citric acid (H(4)cit) in acetonitrile solution to provide the chelate derivative [GeCl(bipy)(Hcit)] (II). The structures of compounds I and II have been determined by single crystal X-ray diffraction. For I the central germanium shows octahedral geometry with two mutually cis-chlorine atoms, Ge-Cl (mean) 2.244(1) Angstrom, and the bidentate ligand, Ge-N (mean) 2.065(4) Angstrom occupying equatorial positions and two mutually tuans-chlorine atoms, Ge-Cl (mean) 2.267(1) Angstrom in axial locations. For II the citrate ligand is terdentate and bound to the central germanium via its hydroxyl, alpha -carboxylate and one of the beta -carboxylate groups in a fac-octahedral arrangement. Ge-O-hydroxyl 1.800(3) Angstrom, Ge-O-carboxylate (mean) 1.904(3) Angstrom, Ge-Cl 2.209(1) Angstrom, Ge-N (mean) 2.012(3) Angstrom. The uncoordinated P-carboxylate group remains intact as a 'dangling arm'. The structure also contains poorly defined and disordered acetonitrile (solvent) molecules trapped in the lattice. (C) 2001 Elsevier Science B.V. All rights reserved.
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页码:191 / 195
页数:5
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